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Showing results (191-200 of 196) with videos related to

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Diabetologia|February 1, 1997
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 familiesG Velho, H Blanché, M Vaxillaire, et al.
Human Molecular Genetics|April 1, 1997
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)M Vaxillaire, M Rouard, K Yamagata, et al.
Annals of Internal Medicine|May 1, 2001
Maternally inherited diabetes and deafness: a multicenter studyP J Guillausseau, P Massin, D Dubois-LaForgue, et al.
Diabetes & Metabolism|June 30, 2004
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)P J Guillausseau, D Dubois-Laforgue, P Massin, et al.
Diabetologia|June 27, 2008
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control studyP Massin, D Dubois-Laforgue, T Meas, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2009
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytesM Laloi-Michelin, T Meas, C Ambonville, et al.
Pageof 20

Showing results (191-200 of 196) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 196 results.
Diabetologia|February 1, 1997
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 familiesG Velho, H Blanché, M Vaxillaire, et al.
Human Molecular Genetics|April 1, 1997
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)M Vaxillaire, M Rouard, K Yamagata, et al.
Annals of Internal Medicine|May 1, 2001
Maternally inherited diabetes and deafness: a multicenter studyP J Guillausseau, P Massin, D Dubois-LaForgue, et al.
Diabetes & Metabolism|June 30, 2004
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)P J Guillausseau, D Dubois-Laforgue, P Massin, et al.
Diabetologia|June 27, 2008
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control studyP Massin, D Dubois-Laforgue, T Meas, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2009
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytesM Laloi-Michelin, T Meas, C Ambonville, et al.
Pageof 20